| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6657442 | 1.000 | 0.040 | 1 | 196868930 | intron variant | T/C | snv | 0.19 | 2 | ||
| rs6677604 | 0.827 | 0.200 | 1 | 196717788 | intron variant | G/A | snv | 0.23 | 2 | ||
| rs7366238 | 1.000 | 0.040 | 1 | 196891667 | intron variant | A/G | snv | 0.22 | 2 | ||
| rs7413265 | 1.000 | 0.040 | 1 | 196870033 | intron variant | G/T | snv | 0.19 | 2 | ||
| rs7535696 | 1.000 | 0.040 | 1 | 196402302 | intron variant | T/C | snv | 0.27 | 2 | ||
| rs7540032 | 0.925 | 0.080 | 1 | 196732154 | intron variant | C/T | snv | 0.44 | 2 | ||
| rs7555070 | 1.000 | 0.040 | 1 | 197013024 | downstream gene variant | C/T | snv | 0.57 | 2 | ||
| rs1021636 | 1.000 | 0.040 | 1 | 196876143 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs10494745 | 1.000 | 0.040 | 1 | 196918327 | missense variant | G/A | snv | 8.0E-02 | 7.4E-02 | 1 | |
| rs1061147 | 1.000 | 0.040 | 1 | 196685194 | synonymous variant | A/C | snv | 0.68 | 0.62 | 1 | |
| rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 1 | |
| rs10733086 | 1.000 | 0.040 | 1 | 196707805 | intron variant | A/C;T | snv | 1 | |||
| rs10754196 | 1.000 | 0.040 | 1 | 196601576 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs10754198 | 1.000 | 0.040 | 1 | 196604375 | intron variant | A/T | snv | 0.30 | 1 | ||
| rs10754199 | 1.000 | 0.040 | 1 | 196701709 | intron variant | A/G | snv | 0.64 | 1 | ||
| rs10754206 | 1.000 | 0.040 | 1 | 196851794 | intron variant | T/G | snv | 0.41 | 1 | ||
| rs10801553 | 1.000 | 0.040 | 1 | 196686613 | intron variant | A/C | snv | 0.64 | 1 | ||
| rs10801554 | 1.000 | 0.040 | 1 | 196688525 | intron variant | C/T | snv | 0.64 | 1 | ||
| rs10801555 | 1.000 | 0.040 | 1 | 196691131 | intron variant | A/G | snv | 0.64 | 1 | ||
| rs10801556 | 1.000 | 0.040 | 1 | 196691334 | intron variant | A/G | snv | 0.64 | 1 | ||
| rs10801575 | 1.000 | 0.040 | 1 | 196883651 | intron variant | T/A;C | snv | 1 | |||
| rs10801580 | 1.000 | 0.040 | 1 | 196916555 | non coding transcript exon variant | T/C | snv | 0.21 | 1 | ||
| rs10922082 | 1.000 | 0.040 | 1 | 196544564 | intron variant | G/A | snv | 0.30 | 1 | ||
| rs10922083 | 1.000 | 0.040 | 1 | 196547268 | intron variant | C/A;T | snv | 1 | |||
| rs10922084 | 1.000 | 0.040 | 1 | 196556184 | intron variant | A/C | snv | 0.30 | 1 |